TWI426904B - 1,1,1-三氟-2-羥基-3-苯丙烷衍生物 - Google Patents
1,1,1-三氟-2-羥基-3-苯丙烷衍生物 Download PDFInfo
- Publication number
- TWI426904B TWI426904B TW097137403A TW97137403A TWI426904B TW I426904 B TWI426904 B TW I426904B TW 097137403 A TW097137403 A TW 097137403A TW 97137403 A TW97137403 A TW 97137403A TW I426904 B TWI426904 B TW I426904B
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- Prior art keywords
- phenyl
- trifluoro
- chloro
- methyl
- pyridin
- Prior art date
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- UPFLNTYTTUCHQN-UHFFFAOYSA-N 1,1,1-trifluoro-3-phenylpropan-2-ol Chemical class FC(F)(F)C(O)CC1=CC=CC=C1 UPFLNTYTTUCHQN-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 349
- -1 C 1-7 -alkyl Chemical class 0.000 claims description 203
- 229910052736 halogen Inorganic materials 0.000 claims description 71
- 150000002367 halogens Chemical class 0.000 claims description 56
- 125000004076 pyridyl group Chemical group 0.000 claims description 52
- 125000001424 substituent group Chemical group 0.000 claims description 47
- 229910052739 hydrogen Inorganic materials 0.000 claims description 44
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 44
- 239000001257 hydrogen Substances 0.000 claims description 43
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 35
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 31
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 31
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 28
- 125000005843 halogen group Chemical group 0.000 claims description 24
- 125000001072 heteroaryl group Chemical group 0.000 claims description 23
- 102000007451 Steroid Receptors Human genes 0.000 claims description 22
- 108091008723 corticosteroid receptors Proteins 0.000 claims description 22
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 21
- 238000011282 treatment Methods 0.000 claims description 20
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 201000010099 disease Diseases 0.000 claims description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 14
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 150000002431 hydrogen Chemical class 0.000 claims description 12
- 125000000335 thiazolyl group Chemical group 0.000 claims description 12
- 239000005711 Benzoic acid Substances 0.000 claims description 11
- 206010012601 diabetes mellitus Diseases 0.000 claims description 11
- 239000003814 drug Substances 0.000 claims description 11
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 11
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 11
- 125000005493 quinolyl group Chemical group 0.000 claims description 11
- 150000002923 oximes Chemical class 0.000 claims description 10
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 10
- 125000006701 (C1-C7) alkyl group Chemical group 0.000 claims description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 9
- DGPKWPAJWGEIPS-UHFFFAOYSA-N 4-[3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]-1h-pyridin-2-one Chemical compound C1=CNC(=O)C=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl DGPKWPAJWGEIPS-UHFFFAOYSA-N 0.000 claims description 8
- 125000003943 azolyl group Chemical group 0.000 claims description 8
- 125000002720 diazolyl group Chemical group 0.000 claims description 8
- 125000001041 indolyl group Chemical group 0.000 claims description 8
- PKAUVIXBZJUYRV-UHFFFAOYSA-N methane;hydroiodide Chemical compound C.I PKAUVIXBZJUYRV-UHFFFAOYSA-N 0.000 claims description 8
- 125000001113 thiadiazolyl group Chemical group 0.000 claims description 8
- VZNZZHAOGLCMAS-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyridin-4-ylbutan-2-ol Chemical compound C=1C=NC=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl VZNZZHAOGLCMAS-UHFFFAOYSA-N 0.000 claims description 7
- PJTYQUYHHUYARD-UHFFFAOYSA-N 5-[3-(2-chloro-4-hydroxyphenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]-1-methylpyridin-2-one Chemical compound C1=CC(=O)N(C)C=C1C(O)(C(F)(F)F)C(C)C1=CC=C(O)C=C1Cl PJTYQUYHHUYARD-UHFFFAOYSA-N 0.000 claims description 7
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 7
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims description 7
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 7
- KQANPJTZUJVNMJ-UHFFFAOYSA-N 3-(2-chloro-5-methoxyphenyl)-2-(2-chloropyridin-4-yl)-1,1,1-trifluorobutan-2-ol Chemical compound COC1=CC=C(Cl)C(C(C)C(O)(C=2C=C(Cl)N=CC=2)C(F)(F)F)=C1 KQANPJTZUJVNMJ-UHFFFAOYSA-N 0.000 claims description 6
- CIEQMWBGCGRGPH-UHFFFAOYSA-N 5-[3-(2,3-dichloro-4-methoxyphenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]-1-methylpyridin-2-one Chemical compound ClC1=C(Cl)C(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CN(C)C(=O)C=C1 CIEQMWBGCGRGPH-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- IAVQXROAGOOBDO-UHFFFAOYSA-N 2,2-dimethyl-3-(trifluoromethyl)decane Chemical compound FC(F)(F)C(C(C)(C)C)CCCCCCC IAVQXROAGOOBDO-UHFFFAOYSA-N 0.000 claims description 5
- WMMQOHORDOZVGR-UHFFFAOYSA-N 3-(2-chloro-4-fluorophenyl)-1,1,1-trifluoro-2-(2-iodopyridin-4-yl)butan-2-ol Chemical compound C=1C=NC(I)=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(F)C=C1Cl WMMQOHORDOZVGR-UHFFFAOYSA-N 0.000 claims description 5
- LZTRYSZGZKNRNX-UHFFFAOYSA-N 3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-(2-methylpyridin-4-yl)butan-2-ol Chemical compound ClC1=CC(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CC=NC(C)=C1 LZTRYSZGZKNRNX-UHFFFAOYSA-N 0.000 claims description 5
- WLZPNPKQWOLHJA-UHFFFAOYSA-N 3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-pyrazolo[1,5-a]pyridin-3-ylbutan-2-ol Chemical compound ClC1=CC(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=C2C=CC=CN2N=C1 WLZPNPKQWOLHJA-UHFFFAOYSA-N 0.000 claims description 5
- ORFSLHLRWXMAJM-UHFFFAOYSA-N 3-[2-chloro-4-(hydroxymethyl)phenyl]-2-(2-chloropyridin-4-yl)-1,1,1-trifluorobutan-2-ol Chemical compound C=1C=NC(Cl)=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(CO)C=C1Cl ORFSLHLRWXMAJM-UHFFFAOYSA-N 0.000 claims description 5
- SVBYFSRMFQUKSC-UHFFFAOYSA-N 3-[3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]quinoline-6-carbonitrile Chemical compound ClC1=CC(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CN=C(C=CC(=C2)C#N)C2=C1 SVBYFSRMFQUKSC-UHFFFAOYSA-N 0.000 claims description 5
- OXRDLXYKVKXEOF-UHFFFAOYSA-N 5-[3-(4-bromo-2-chlorophenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]-1h-pyridin-2-one Chemical compound C1=CC(=O)NC=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Br)C=C1Cl OXRDLXYKVKXEOF-UHFFFAOYSA-N 0.000 claims description 5
- 125000005946 imidazo[1,2-a]pyridyl group Chemical group 0.000 claims description 5
- 230000002265 prevention Effects 0.000 claims description 5
- STVRBHCAMGAPBF-UHFFFAOYSA-N 1,1,1-trifluoro-3-(2-phenoxyphenyl)-2-pyridin-4-ylbutan-2-ol Chemical compound C=1C=NC=CC=1C(O)(C(F)(F)F)C(C)C1=CC=CC=C1OC1=CC=CC=C1 STVRBHCAMGAPBF-UHFFFAOYSA-N 0.000 claims description 4
- GBHFWDNFAPDIKA-UHFFFAOYSA-N 1-[1-(2,4-dichlorophenyl)cyclopropyl]-2,2,2-trifluoro-1-quinolin-3-ylethanol Chemical compound C=1N=C2C=CC=CC2=CC=1C(O)(C(F)(F)F)C1(C=2C(=CC(Cl)=CC=2)Cl)CC1 GBHFWDNFAPDIKA-UHFFFAOYSA-N 0.000 claims description 4
- GDCCHNWFECUDNF-UHFFFAOYSA-N 1-[1-(4-chlorophenyl)cyclopropyl]-2,2,2-trifluoro-1-quinolin-3-ylethanol Chemical compound C=1N=C2C=CC=CC2=CC=1C(O)(C(F)(F)F)C1(C=2C=CC(Cl)=CC=2)CC1 GDCCHNWFECUDNF-UHFFFAOYSA-N 0.000 claims description 4
- PCPCOCRDFPUQLC-UHFFFAOYSA-N 2-(2-chloro-6-methylpyridin-4-yl)-3-(2,4-dichlorophenyl)-1,1,1-trifluorobutan-2-ol Chemical compound C=1C(C)=NC(Cl)=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl PCPCOCRDFPUQLC-UHFFFAOYSA-N 0.000 claims description 4
- LSXHHPJSZHIMMR-UHFFFAOYSA-N 2-(2-chloropyridin-4-yl)-3-(2,4-dichlorophenyl)-1,1,1-trifluoro-3-methylbutan-2-ol Chemical compound C=1C=NC(Cl)=CC=1C(O)(C(F)(F)F)C(C)(C)C1=CC=C(Cl)C=C1Cl LSXHHPJSZHIMMR-UHFFFAOYSA-N 0.000 claims description 4
- OXHXPTRLOBVHGS-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(2-methoxypyridin-4-yl)butan-2-ol Chemical compound C1=NC(OC)=CC(C(O)(C(C)C=2C(=CC(Cl)=CC=2)Cl)C(F)(F)F)=C1 OXHXPTRLOBVHGS-UHFFFAOYSA-N 0.000 claims description 4
- XTMCUXBKIABCDL-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(2-methylpyridin-4-yl)butan-2-ol Chemical compound C=1C=NC(C)=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl XTMCUXBKIABCDL-UHFFFAOYSA-N 0.000 claims description 4
- VDSQTSOWOWMKSC-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(5-fluoro-1h-indol-3-yl)butan-2-ol Chemical compound C=1NC2=CC=C(F)C=C2C=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl VDSQTSOWOWMKSC-UHFFFAOYSA-N 0.000 claims description 4
- MWQWAYLOBAFGSS-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-quinolin-3-ylbutan-2-ol Chemical compound C=1N=C2C=CC=CC2=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl MWQWAYLOBAFGSS-UHFFFAOYSA-N 0.000 claims description 4
- HTUKMHBAGIZIFY-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-quinolin-6-ylbutan-2-ol Chemical compound C=1C=C2N=CC=CC2=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl HTUKMHBAGIZIFY-UHFFFAOYSA-N 0.000 claims description 4
- VHRXBEXIYBXIQT-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-quinoxalin-6-ylbutan-2-ol Chemical compound C=1C=C2N=CC=NC2=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl VHRXBEXIYBXIQT-UHFFFAOYSA-N 0.000 claims description 4
- IYPZQOZYSWIHOM-UHFFFAOYSA-N 3-(2-chloro-4-ethoxyphenyl)-1,1,1-trifluoro-2-(2-methylpyridin-4-yl)pentan-2-ol Chemical compound ClC1=CC(OCC)=CC=C1C(CC)C(O)(C(F)(F)F)C1=CC=NC(C)=C1 IYPZQOZYSWIHOM-UHFFFAOYSA-N 0.000 claims description 4
- HIJJJMKHJBECJI-UHFFFAOYSA-N 3-(2-chloro-4-fluorophenyl)-2-(2-chloro-6-methoxypyridin-4-yl)-1,1,1-trifluorobutan-2-ol Chemical compound ClC1=NC(OC)=CC(C(O)(C(C)C=2C(=CC(F)=CC=2)Cl)C(F)(F)F)=C1 HIJJJMKHJBECJI-UHFFFAOYSA-N 0.000 claims description 4
- FXVUNOIPELGISW-UHFFFAOYSA-N 3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-(2-iodopyridin-4-yl)butan-2-ol Chemical compound ClC1=CC(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CC=NC(I)=C1 FXVUNOIPELGISW-UHFFFAOYSA-N 0.000 claims description 4
- ZPVMAZZJSOVJNW-UHFFFAOYSA-N 3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-isoquinolin-5-ylbutan-2-ol Chemical compound ClC1=CC(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CC=CC2=CN=CC=C12 ZPVMAZZJSOVJNW-UHFFFAOYSA-N 0.000 claims description 4
- JDMXGTUXLOKVMW-UHFFFAOYSA-N 3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-pyridin-4-ylbutan-2-ol Chemical compound ClC1=CC(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CC=NC=C1 JDMXGTUXLOKVMW-UHFFFAOYSA-N 0.000 claims description 4
- IVNCDYJFRMCQMP-UHFFFAOYSA-N 3-(2-chloro-4-methoxyphenyl)-2-(2-chloropyridin-4-yl)-1,1,1-trifluorobutan-2-ol Chemical compound ClC1=CC(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CC=NC(Cl)=C1 IVNCDYJFRMCQMP-UHFFFAOYSA-N 0.000 claims description 4
- PAKBIRMXJYSOBB-UHFFFAOYSA-N 3-(4-bromo-2-chlorophenyl)-1,1,1-trifluoro-2-(6-methoxypyridin-3-yl)butan-2-ol Chemical compound C1=NC(OC)=CC=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Br)C=C1Cl PAKBIRMXJYSOBB-UHFFFAOYSA-N 0.000 claims description 4
- LPRVJPJXWVMFPD-UHFFFAOYSA-N 3-chloro-4-[3-(2-chloropyridin-4-yl)-4,4,4-trifluoro-3-hydroxybutan-2-yl]phenol Chemical compound C=1C=NC(Cl)=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(O)C=C1Cl LPRVJPJXWVMFPD-UHFFFAOYSA-N 0.000 claims description 4
- SEDLXEIRMUVECG-UHFFFAOYSA-N 5-[3-(4-bromo-2-chlorophenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]-1-ethylpyridin-2-one Chemical compound C1=CC(=O)N(CC)C=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Br)C=C1Cl SEDLXEIRMUVECG-UHFFFAOYSA-N 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- HTUKMHBAGIZIFY-ADLMAVQZSA-N (2r,3r)-3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-quinolin-6-ylbutan-2-ol Chemical compound C1([C@@H](C)[C@@](O)(C=2C=C3C=CC=NC3=CC=2)C(F)(F)F)=CC=C(Cl)C=C1Cl HTUKMHBAGIZIFY-ADLMAVQZSA-N 0.000 claims description 3
- HTUKMHBAGIZIFY-VOJFVSQTSA-N (2s,3s)-3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-quinolin-6-ylbutan-2-ol Chemical compound C1([C@H](C)[C@](O)(C=2C=C3C=CC=NC3=CC=2)C(F)(F)F)=CC=C(Cl)C=C1Cl HTUKMHBAGIZIFY-VOJFVSQTSA-N 0.000 claims description 3
- DNLLBMOCMFJWRZ-UHFFFAOYSA-N 2-(1-benzylpyrazol-4-yl)-3-(2,4-dichlorophenyl)-1,1,1-trifluorobutan-2-ol Chemical compound C1=NN(CC=2C=CC=CC=2)C=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl DNLLBMOCMFJWRZ-UHFFFAOYSA-N 0.000 claims description 3
- IEVOVLLHJZOIIK-UHFFFAOYSA-N 2-(6-chloropyridin-3-yl)-3-(2,4-dichlorophenyl)-1,1,1-trifluorobutan-2-ol Chemical compound C=1C=C(Cl)N=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl IEVOVLLHJZOIIK-UHFFFAOYSA-N 0.000 claims description 3
- DEBIDWSURWRZDI-UHFFFAOYSA-N 2-[4-[3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]pyridin-2-yl]oxyacetamide Chemical compound C=1C=NC(OCC(N)=O)=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl DEBIDWSURWRZDI-UHFFFAOYSA-N 0.000 claims description 3
- MKZAZGGHARXTLB-UHFFFAOYSA-N 2-[4-[3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]pyridin-2-yl]oxyacetonitrile Chemical compound C=1C=NC(OCC#N)=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl MKZAZGGHARXTLB-UHFFFAOYSA-N 0.000 claims description 3
- XYHASIYPDSRWOO-UHFFFAOYSA-N 3-(2,3-dichlorophenyl)-1,1,1-trifluoro-2-pyridin-3-ylbutan-2-ol Chemical compound C=1C=CN=CC=1C(O)(C(F)(F)F)C(C)C1=CC=CC(Cl)=C1Cl XYHASIYPDSRWOO-UHFFFAOYSA-N 0.000 claims description 3
- UBPHTGIDQKLEDP-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(1-methylpyrazol-3-yl)butan-2-ol Chemical compound C1=CN(C)N=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl UBPHTGIDQKLEDP-UHFFFAOYSA-N 0.000 claims description 3
- RNRHKAFBOZUGKJ-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(1-methylpyrazol-4-yl)butan-2-ol Chemical compound C1=NN(C)C=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl RNRHKAFBOZUGKJ-UHFFFAOYSA-N 0.000 claims description 3
- OGCPPTJTSLJVGB-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(1-phenylindazol-5-yl)butan-2-ol Chemical compound C=1C=C2N(C=3C=CC=CC=3)N=CC2=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl OGCPPTJTSLJVGB-UHFFFAOYSA-N 0.000 claims description 3
- GQMSZEZQTAMSPH-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(2-methylpyridin-4-yl)hexan-2-ol Chemical compound C=1C=NC(C)=CC=1C(O)(C(F)(F)F)C(CCC)C1=CC=C(Cl)C=C1Cl GQMSZEZQTAMSPH-UHFFFAOYSA-N 0.000 claims description 3
- SSTRBSNUXMOGGE-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(6-methoxypyridin-3-yl)butan-2-ol Chemical compound C1=NC(OC)=CC=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl SSTRBSNUXMOGGE-UHFFFAOYSA-N 0.000 claims description 3
- GTVKYLZGRHRZFF-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyrazolo[1,5-a]pyridin-3-ylbutan-2-ol Chemical compound C1=NN2C=CC=CC2=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl GTVKYLZGRHRZFF-UHFFFAOYSA-N 0.000 claims description 3
- WTKRHZUGRRCZEV-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyridin-2-ylbutan-2-ol Chemical compound C=1C=CC=NC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl WTKRHZUGRRCZEV-UHFFFAOYSA-N 0.000 claims description 3
- ZNVOGUXVGZAVSQ-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyridin-3-ylbutan-2-ol Chemical compound C=1C=CN=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl ZNVOGUXVGZAVSQ-UHFFFAOYSA-N 0.000 claims description 3
- NLIPMCLKYJDHEF-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyridin-3-ylheptan-2-ol Chemical compound C=1C=CN=CC=1C(O)(C(F)(F)F)C(CCCC)C1=CC=C(Cl)C=C1Cl NLIPMCLKYJDHEF-UHFFFAOYSA-N 0.000 claims description 3
- AETBIWSIEYWXRL-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyridin-3-ylhexan-2-ol Chemical compound C=1C=CN=CC=1C(O)(C(F)(F)F)C(CCC)C1=CC=C(Cl)C=C1Cl AETBIWSIEYWXRL-UHFFFAOYSA-N 0.000 claims description 3
- IHBDYHLDHFUIDK-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyridin-4-ylhexan-2-ol Chemical compound C=1C=NC=CC=1C(O)(C(F)(F)F)C(CCC)C1=CC=C(Cl)C=C1Cl IHBDYHLDHFUIDK-UHFFFAOYSA-N 0.000 claims description 3
- LYYQABAXPWTELG-UHFFFAOYSA-N 3-(2,5-dichlorophenyl)-1,1,1-trifluoro-2-(2-methylpyridin-4-yl)butan-2-ol Chemical compound C=1C=NC(C)=CC=1C(O)(C(F)(F)F)C(C)C1=CC(Cl)=CC=C1Cl LYYQABAXPWTELG-UHFFFAOYSA-N 0.000 claims description 3
- PRJIQKBRODCQJN-UHFFFAOYSA-N 3-(2-chloro-4-fluorophenyl)-1,1,1-trifluoro-2-(2-methoxypyridin-4-yl)butan-2-ol Chemical compound C1=NC(OC)=CC(C(O)(C(C)C=2C(=CC(F)=CC=2)Cl)C(F)(F)F)=C1 PRJIQKBRODCQJN-UHFFFAOYSA-N 0.000 claims description 3
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- QDCLSKWCDAUEAC-UHFFFAOYSA-N 4-[4-[3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]pyridin-2-yl]benzoic acid Chemical compound ClC1=CC(OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CC=NC(C=2C=CC(=CC=2)C(O)=O)=C1 QDCLSKWCDAUEAC-UHFFFAOYSA-N 0.000 claims description 3
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- CFWFEPUDFUHMMQ-UHFFFAOYSA-N methyl 3-[4-[3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]pyridin-2-yl]benzoate Chemical compound COC(=O)C1=CC=CC(C=2N=CC=C(C=2)C(O)(C(C)C=2C(=CC(OC)=CC=2)Cl)C(F)(F)F)=C1 CFWFEPUDFUHMMQ-UHFFFAOYSA-N 0.000 claims description 3
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- KIBOFPYOXNHDTA-UHFFFAOYSA-N 2-[4-[3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]-2-oxopyridin-1-yl]acetic acid Chemical compound C1=CN(CC(O)=O)C(=O)C=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl KIBOFPYOXNHDTA-UHFFFAOYSA-N 0.000 claims description 2
- ZCEABLAANPSVFJ-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-(1,3-thiazol-2-yl)butan-2-ol Chemical compound N=1C=CSC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl ZCEABLAANPSVFJ-UHFFFAOYSA-N 0.000 claims description 2
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- DDYCMJCMVBGJMK-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-[1-(3-methoxyphenyl)indazol-5-yl]butan-2-ol Chemical compound COC1=CC=CC(N2C3=CC=C(C=C3C=N2)C(O)(C(C)C=2C(=CC(Cl)=CC=2)Cl)C(F)(F)F)=C1 DDYCMJCMVBGJMK-UHFFFAOYSA-N 0.000 claims description 2
- JEZKOFNPYLTBQG-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-[1-(4-methoxyphenyl)indazol-5-yl]butan-2-ol Chemical compound C1=CC(OC)=CC=C1N1C2=CC=C(C(O)(C(C)C=3C(=CC(Cl)=CC=3)Cl)C(F)(F)F)C=C2C=N1 JEZKOFNPYLTBQG-UHFFFAOYSA-N 0.000 claims description 2
- GDMHGYMORQNAGB-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyrazolo[1,5-a]pyridin-2-ylbutan-2-ol Chemical compound C1=C2C=CC=CN2N=C1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl GDMHGYMORQNAGB-UHFFFAOYSA-N 0.000 claims description 2
- VUAQLNNNTNFXNE-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-pyrimidin-4-ylbutan-2-ol Chemical compound C=1C=NC=NC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl VUAQLNNNTNFXNE-UHFFFAOYSA-N 0.000 claims description 2
- LUOGJMMHAREPHE-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-quinoxalin-2-ylbutan-2-ol Chemical compound C=1N=C2C=CC=CC2=NC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl LUOGJMMHAREPHE-UHFFFAOYSA-N 0.000 claims description 2
- LCZVNMBHXUCMFG-UHFFFAOYSA-N 3-(2,4-difluorophenyl)-1,1,1-trifluoro-2-pyridin-4-ylbutan-2-ol Chemical compound C=1C=NC=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(F)C=C1F LCZVNMBHXUCMFG-UHFFFAOYSA-N 0.000 claims description 2
- PSLLSOKFKOLKIL-UHFFFAOYSA-N 3-(2-chlorophenyl)-1,1,1-trifluoro-2-pyridin-3-ylbutan-2-ol Chemical compound C=1C=CN=CC=1C(O)(C(F)(F)F)C(C)C1=CC=CC=C1Cl PSLLSOKFKOLKIL-UHFFFAOYSA-N 0.000 claims description 2
- JQAXJXUAHBWTLT-UHFFFAOYSA-N 3-[2-chloro-4-[(4-methylsulfonylphenyl)methoxy]phenyl]-1,1,1-trifluoro-2-quinolin-3-ylbutan-2-ol Chemical compound C=1N=C2C=CC=CC2=CC=1C(O)(C(F)(F)F)C(C)C(C(=C1)Cl)=CC=C1OCC1=CC=C(S(C)(=O)=O)C=C1 JQAXJXUAHBWTLT-UHFFFAOYSA-N 0.000 claims description 2
- XTSCYZDAVLFQHM-UHFFFAOYSA-N 3-chloro-4-(4,4,4-trifluoro-3-hydroxy-3-pyrazolo[1,5-a]pyridin-3-ylbutan-2-yl)phenol Chemical compound C1=NN2C=CC=CC2=C1C(O)(C(F)(F)F)C(C)C1=CC=C(O)C=C1Cl XTSCYZDAVLFQHM-UHFFFAOYSA-N 0.000 claims description 2
- BFONTBDEXUCPJT-UHFFFAOYSA-N CC(C1=C(C=C(C=C1)Cl)Cl)C(C2=CC(=O)N(C=C2)COC(=O)C)(C(F)(F)F)O Chemical compound CC(C1=C(C=C(C=C1)Cl)Cl)C(C2=CC(=O)N(C=C2)COC(=O)C)(C(F)(F)F)O BFONTBDEXUCPJT-UHFFFAOYSA-N 0.000 claims description 2
- OWDAVYVJYLIDNJ-UHFFFAOYSA-N ethyl 4-[4-[3-(2-chloro-4-methoxyphenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]pyridin-2-yl]benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1C1=CC(C(O)(C(C)C=2C(=CC(OC)=CC=2)Cl)C(F)(F)F)=CC=N1 OWDAVYVJYLIDNJ-UHFFFAOYSA-N 0.000 claims description 2
- AAHFYBIWTZHJBP-UHFFFAOYSA-N methyl 4-[3-(2-chloro-4-methoxycarbonylphenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]pyridine-2-carboxylate Chemical compound ClC1=CC(C(=O)OC)=CC=C1C(C)C(O)(C(F)(F)F)C1=CC=NC(C(=O)OC)=C1 AAHFYBIWTZHJBP-UHFFFAOYSA-N 0.000 claims description 2
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- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- DUHFHQKINZOLNB-UHFFFAOYSA-N tert-butyl 7-[3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]-3,4-dihydro-1h-isoquinoline-2-carboxylate Chemical compound C=1C=C2CCN(C(=O)OC(C)(C)C)CC2=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl DUHFHQKINZOLNB-UHFFFAOYSA-N 0.000 claims description 2
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- RPSQKWQFZVDNLG-UHFFFAOYSA-N 4-[5-[3-(2,4-dichlorophenyl)-1,1,1-trifluoro-2-hydroxybutan-2-yl]indazol-1-yl]phenol Chemical compound C=1C=C2N(C=3C=CC(O)=CC=3)N=CC2=CC=1C(O)(C(F)(F)F)C(C)C1=CC=C(Cl)C=C1Cl RPSQKWQFZVDNLG-UHFFFAOYSA-N 0.000 claims 1
- QPJVMBTYPHYUOC-UHFFFAOYSA-N Methyl benzoate Natural products COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 claims 1
- 230000002152 alkylating effect Effects 0.000 claims 1
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- 125000005842 heteroatom Chemical group 0.000 claims 1
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 claims 1
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- 229960004699 valsartan Drugs 0.000 description 1
- SYOKIDBDQMKNDQ-XWTIBIIYSA-N vildagliptin Chemical compound C1C(O)(C2)CC(C3)CC1CC32NCC(=O)N1CCC[C@H]1C#N SYOKIDBDQMKNDQ-XWTIBIIYSA-N 0.000 description 1
- 229960001254 vildagliptin Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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- 238000005406 washing Methods 0.000 description 1
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- 239000000080 wetting agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
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Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/12—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D215/14—Radicals substituted by oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
- C07D217/14—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
- C07D217/16—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals substituted by oxygen atoms
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- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
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- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
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- C—CHEMISTRY; METALLURGY
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- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- Medicinal Chemistry (AREA)
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- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Quinoline Compounds (AREA)
- Indole Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
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| EP07117360 | 2007-09-27 |
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| TW200914005A TW200914005A (en) | 2009-04-01 |
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| TW097137403A TWI426904B (zh) | 2007-09-27 | 2008-09-26 | 1,1,1-三氟-2-羥基-3-苯丙烷衍生物 |
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| JP (1) | JP5242691B2 (pl) |
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| WO2010049073A1 (en) * | 2008-10-30 | 2010-05-06 | Bayer Schering Pharma Aktiengesellschaft | 1,1,1-trifluoro-3-amino-3-heteroaryl-2-propanoles, a process for their production and their use as anti-inflammatory agents |
| US8138189B2 (en) * | 2009-03-26 | 2012-03-20 | Hoffman-La Roche Inc. | Substituted benzene compounds as modulators of the glucocorticoid receptor |
| JP5408415B2 (ja) * | 2009-06-10 | 2014-02-05 | Jsr株式会社 | 1位置換3,5−ジアミノベンゼンの製造方法 |
| PH12012501104A1 (en) * | 2009-12-04 | 2014-10-14 | Nissan Chemical Ind Ltd | 2-pyridone compounds |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| US9056855B2 (en) * | 2010-10-28 | 2015-06-16 | Viamet Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| KR102251681B1 (ko) * | 2013-08-23 | 2021-05-14 | 바스프 에스이 | 말단 헤테로아릴시아노비닐렌 기를 갖는 화합물 및 이의 유기 태양 전지에서의 용도 |
| JP6048533B2 (ja) * | 2014-05-12 | 2016-12-21 | 日産化学工業株式会社 | 2−ピリドン化合物を含有する医薬 |
| CA3082558A1 (en) * | 2017-11-16 | 2019-05-23 | Syngenta Participations Ag | Process for the preparation of enantiomerically and diastereomerically enriched cyclobutane amines and amides |
| US10450022B2 (en) | 2018-01-31 | 2019-10-22 | David Watson | Device for adjusting a seat position of a bicycle seat |
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| WO2006135826A1 (en) * | 2005-06-10 | 2006-12-21 | Boehringer Ingelheim International Gmbh | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
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